HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412962Generated: October 29, 2026
Ammonium Chloride → HCID 18537395, compound
https://huagongshe.com/reaction/412962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 18536857 | HCID 18536857 | — |
| Reactant | HCID 18537416 | HCID 18537416 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 18537395 | HCID 18537395 | 44% |
Reaction Steps
4-[4-(3-Hydroxy-4-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxamidine hydrochiloride: A portion of the mixture (320 mg, ca. 0.788 mmol as based on the 1H-NMR spectrum) containing the 2-methoxy-5-{2-[5-(methoxvcarbonyl)-2-methylthio(3-thienyl)](1,3-thiazol-4-yl)}phenyl acetate (as prepared in the previous step) was treated according to the procedure in Example 10, step (b), using 415 mg (7.76 mmol) of ammonium chloride in 3.5 mL of toluene and 3.88 mL (7.66 mmol) of 2 M trimethylaluminum in toluene. After chromatography of the resulting residue on a 10 g silica SPE column (Waters Sep-Pak) with 10-40% MeOH-CH2Cl2, a light yellow solid was obtained which was dissolved in 45 mL of DMF and filtered to remove silica gel. Concentration under high vacuum and recrystallization from MeOH—Et2O afforded the title compound as a light tan solid (132 mg, 44%). 1H-NMR (300 MHz, DMSO-d6) δ 9.49 (broad s, 2H), 9.16 (broad s, 2H), 8.67 (s, 1H), 7.98 (s, 1H), 7.5 (obscured m, 3H), 7.00 (obscured d, 1H, J=8.3 Hz), 3.82 (s, 3H), and 2.79 (s, 3H). Mass spectrum (ESI) calcd. for C16H15N3O2S3: 378.0 (M+H). Found: 378.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562840B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-b225de112ae34addab584105b1e950a5 |
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| Source note | uspto-grants-2003_05 |
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